Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999604-175000383 | Common:4; Rare:271 | ||||
chr1:175023394-175023517 | Common:1; Rare:38 | ||||
chr1:175192661-175193109 | Common:5; Rare:125 | ||||
chr1:175193113-175193321 | Common:2; Rare:31 | ||||
chr1:176207220-176207345 | Common:2; Rare:63 | ||||
chr1:178093601-178093807 | Common:3; Rare:67 | ||||
chr1:178094195-178094493 | Rare:103 | ||||
chr1:178725061-178725367 | Common:10; Rare:110 | ||||
chr1:178869186-178869339 | Common:1; Rare:24 | ||||
chr1:178871016-178871056 | Rare:6 | ||||
chr1:178871059-178871114 | Rare:7 | ||||
chr1:179081911-179082119 | Common:1; Rare:66 | ||||
chr1:179882155-179882364 | Common:1; Rare:43 | ||||
chr1:179882482-179882940 | Common:1; Rare:225; Clinvar:9; Clinvar (benign):4 | ||||
chr1:179954500-179955117 | Common:3; Rare:140 |